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Biomedical subjects

M Marek

Publications and source records attributed to M Marek.

17 recordsLinked to original sources

Interactions between dental amalgams and the oral environment.

Dental amalgam fillings interact in a complex way with the environment in the oral cavity as they are subjected to chemical, biological, mechanical, and thermal forces. These forces change the restoration's appearance and properties, while metal ions, amalgam debris, non-metallic corrosion products, and mercury vapor are released into the oral cavity. The phenomena and conditions that affect the amalgam/environment interaction include the chemistry and biochemistry of the environment, formation of biofilms on the amalgam surfaces, existence of localized corrosion cells, galvanic contacts with other metallic restorations, abrasion during mastication, and synergistic effects of the different forces. Corrosion processes result in a degradation of the functional amalgam properties, while tarnishing reactions cause discoloration. Corrosion degradation of amalgam fillings is due mainly to localized corrosion cells in pores and crevices. Corrosion on occlusal surfaces is accelerated by abrasion during mastication, which removes the protective surface films. The average total amounts of metal species, including mercury, released per day in vivo from a restoration have not been determined. Much of the reported indirect evidence for high mercury release rates is either unreliable or controversial. A more detailed investigation is needed and will require the development of more sophisticated techniques of sampling in vivo, as well as both experimental and theoretical modeling in vitro.

Copper

[A screening method for simultaneous immunochemical detection of aflatoxins and ochratoxin A in cereals and feed].

An immunochemical method was proposed for simultaneous determination of aflatoxin and ochratoxin A with the use of mixed solutions of the following reagents: standards of both mycotoxins, antiserums against the mycotoxins, and radioligands of 125I-aflatoxin B1 and 125I-ochratoxin A. The result of the analytical procedure is the value of concentration of the aflatoxin + ochratoxin A sum in the sample. The procedure needs half the amount of reagents as separate determination of each of the two mycotoxin, and is far less laborious. The proposed simultaneous immunoanalysis is suitable for large-are inspection of grain and feed safety from the viewpoint of aflatoxin and ochratoxin A levels.

Aflatoxins

Corrosion behavior of Pd-Cu and Pd-Co alloys in synthetic saliva.

Pd-based alloys are major alternatives to gold-based alloys for PFM applications. In electrolytes simulating oral fluids, these alloys exhibit electrode behavior similar to passivity of active metals, i.e., a potential region of almost constant current density up to a critical potential, above which the current increases. The objective of this study was to correlate the electrode behavior with the results of solution analyses and changes in the surface composition of the alloys. Binary alloys Pd-15 wt% Cu and Pd-19 wt% Co, as well as the pure components, were examined. Corrosion potentials vs. time, potentiodynamic anodic polarization curves, polarization resistances vs. time, and potentiostatic anodic charges were measured with synthetic saliva used as the electrolyte. The concentrations of Pd, Cu, and Co in the solution after various exposures were determined by atomic absorption. The surfaces of the alloys were examined by x-ray photoelectron spectroscopy before and after the exposures. The results show that selective dissolution of the less-noble components occurred on the surfaces of both alloys for all the exposures, leaving the surfaces highly enriched in Pd. This enrichment contributed to the potential changes and the passive-type behavior. Copper dissolved more than cobalt at longer exposures and higher potentials, in spite of its higher nobility. Dissolution of cobalt seemed to be limited by the formation of a surface film, which may be related to the transition character of this element.

Cobalt

The release of mercury from dental amalgam: the mechanism and in vitro testing.

Dissolution of mercury from the Ag-Hg matrix phase of dental amalgam is distilled water and synthetic saliva, and the mercury evaporation from the solutions, were studied in vitro. The main objectives of the study were to evaluate the factors that affect the results of the mercury release tests, and to consider the possible mechanisms of the release in vivo. Specimens were exposed to the liquids in open or closed bottles, and the changes in the mercury concentration were determined by cold-vapor Atomic Absorption Spectrophotometry. Concentration vs. time tests showed the dissolution rate decreasing with time. Tests involving sequences of short and long exposures with solution changes showed higher average rates for short-term dissolution into the fresh solution than for the longer preceding exposures. The differences were attributed to a stifling effect of the concentration of elemental mercury on the dissolution. It is believed that mercury dissolved mainly in the elemental form and that a continuous increase in the concentration was made possible by oxidation in the solution. In open cells, some of the mercury was lost by evaporation. The analysis showed that the results of mercury dissolution tests depend on many test variables, such as time, solution volume, oxidation and evaporation conditions, etc. Evaporation, dissolution, and evaporation/dissolution mechanisms of the mercury release in vivo were considered. It was concluded that the dissolution/evaporation model best described the mercury release from dental amalgam restorations.

Chemical Phenomena

The effect of tin on the corrosion behavior of the Ag-Hg phase of dental amalgam and dissolution of mercury.

The anodic polarization behavior of the Ag-Hg matrix phase of dental amalgam (gamma 1) and the rate of mercury dissolution were examined as a function of the tin content. The objectives were to determine the effect of tin on the electrochemical behavior and dissolution of mercury and to provide evidence on whether tin dissolves in the gamma 1 phase or precipitates as a tin-rich phase. Anodic polarization curves were recorded for specimens of the gamma 1 phase containing 0-1.5% Sn and for the gamma 2 phase and a gamma 2-containing dental amalgam, in synthetic saliva. Mercury dissolved in synthetic saliva in 24 h was determined for the gamma 1 phase containing 0-1.0% Sn, with cold-vapor Atomic Absorption Spectrophotometry used for mercury analysis. Tin induced passive behavior of the gamma 1 phase and suppressed mercury dissolution. The passive gamma 1 phase did not exhibit a breakdown of passivity occurring at the gamma 2 phase. The results were consistent with the tin presence in gamma 1 in a solid solution, rather than in tin-rich precipitates, and indicated that at least 1.5% Sn can be dissolved in gamma 1 at 37 degrees C.

Corrosion

Corrosion behavior of structural phases in high copper dental amalgam.

The effects of crevice corrosion on the major structural phases of a high copper dental amalgam were studied in vitro. Three kinds of samples were used: (1) amalgam prepared from a high copper, single composition alloy, (2) annealed ingots of the Ag3Sn and Cu3Sn phases, and (3) high copper, single composition alloy tablets electroplated with mercury. Specimens were examined in a scanning electron microscope before and after the exposure to a corrosion environment. The Ag3Sn and Cu3Sn phases were least affected by corrosion. The Ag-Hg-Sn phase (gamma1) slowly deteriorated, but the attack was nonuniform. The Cu6Sn5 phase exhibited good corrosion resistance, better than that of gamma1 phase. Particles of a tin rich phase of uncertain origin were observed on some of the samples after long exposures.

Copper

Spatial structures in a reaction-diffusion system--detailed analysis of the "Brusselator".

Continuous dependence of spatially nonuniform concentration profiles for the 'Brussellator" reaction mechanims on the characteristic length of the system is given both for zero flux and fixed boundary conditions. Branches of solutions arising through primary bifurcation form closed curves. Secondary bifurcations giving rise to spatially asymmetric solutions exist for fixed boundary conditions. Results of a stability analysis of individual solutions are discussed. A method of composing complex spatial profiles for higher lengths from elementary solutions for smaller lenghts is suggested and tested in the case of zero flux boundary conditions. Emergence of subsequently more complex stable patterns in dependence on increasing length of the system suggests many similarities to gradual build up of complex morphogenetic patterns.

Biological Transport

In vitro corrosion of dental amalgam phases.

The effects of corrosion on the major phases of dental amalgam microstructure have been studied in vitro on samples prepared by electroplating mercury on Ag3Sn. Tests were made in synthetic saliva, and samples were examined in a scanning electron microscope before and after the exposure. Simple immersion had little effect on the phases. Contact of amalgam with gold increased the probability of deterioation of the gamma2 phase. By anodic polarization beyond the breakdown potential, the gamma2 phase was selectively dissolved. Under conditions simulating a crevice, the gamma2 phase was dissolved and the gamma1 phase suffered morphological changes.

Corrosion

Synchronization in two interacting oscillatory systems.

Nonlinear phenomena arising from the interaction of two oscillating systems of chemical reactions are studied experimentally. The system of two connected flow-through continuous stirred tank reactors (cells) with controlled exchange of reaction mixture is used. The Belousov reaction (oxidation of malonic acid by bromate in sulphuric acid with ceric/cerous ions as catalyst) served as model system. The frequency of oscillations was controlled by change of the reaction temperature. Phenomena such as synchronization of oscillations at a common frequency, synchronization at multiples of a common frequency, rhythm splitting and amplitude amplification were observed, depending on the degree of interaction and the differences in the original oscillation frequencies. Mathematical modelling of the above phenomena failed, probably due to insufficient knowledge of a kinetic model.

Cell Physiological Phenomena

Nonlinear phenomena in oscillatory systems of homogeneous reactions - experimental observations.

An oscillating system of homogeneous chemical reactions (oxidation of malonic acid by bromate with ceric/cerous ion system as the catalyst) was followed experimentally in several reactor configurations, operated both as close and open systems. Characteristic nonlinear phenomena observed include: damped oscillations of concentrations of reaction components in a well stirred batch reactor, undampted oscillations and sudden changes of oscillatory behaviour (jump to a new steady state) in CSTR and interaction of oscillations in the two connected CSTRs. In a tubular reactor stationary and travelling concentration waves were observed. In the system of CSTR connected with a tubular reactor spreading of waves from CSTR to the tubular reactor, and vice versa was followed. In the flow through tubular reactor the formation of non-monotomic concentration profiles was measured, which were basically stationary with respect to changing flow-rate. The course of oscillations in CSTR was simulated on the basis of a semiempirical reaction kinetics model. An attempt to simulate quantitatively the behaviour of the distributed system with the common type of Fickian diffusion balance equations failed. Difficulties in the proper description of the transport of ions through the concentration gradient and the gradient of the electrical potential found in this system are discussed.

Bromates

New information on high copper amalgam corrosion.

Anodic polarization of "pure" Cu6Sn5 was investigated. Cu6Sn5 is found to be passive in nearly neutral synthetic saliva. Anodic corrosion activity (characteristic for tin) previously reported for a high copper amalgam must result from the presence of the gamma2 phase or tin in the matrix phase.

Chemical Phenomena